Variant #0000000748 (NC_000017.10:g.4851632C>T, PFN1(NM_005022.3):c.58G>A)
| Individual ID |
00000748 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.4851632C>T |
| Reference |
Smith BN1, Vance C1, Scotter EL1, Troakes C1, Wong CH1, Topp S1, Maekawa S1, King A1, Mitchell JC1, Lund K1, Al-Chalabi A1, Ticozzi N2, Silani V2, Sapp P3, Brown RH Jr3, Landers JE3, Al-Sarraj S1, Shaw CE4.(2015) |
| DB-ID |
PFN1_000004 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
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